Canonical Allele Identifier: CA2234889048

Gene: WWOX

Linked Data

• dbSNP Id: rs1165026522
• gnomAD v4: 16-78099747-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78099747G>T , CM000678.2:g.78099747G>T	GRCh38
NC_000016.9:g.78133644G>T , CM000678.1:g.78133644G>T	GRCh37
NC_000016.8:g.76691145G>T	NCBI36
NG_011698.1:g.5094G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.-32G>T	ENSP00000485925.2:n.-32G>T
ENST00000682609.1:n.296G>T
ENST00000683286.1:n.296G>T
ENST00000683929.1:c.-32G>T	ENSP00000507689.1:n.-32G>T
ENST00000684070.1:n.298G>T
ENST00000684381.1:n.296G>T
ENST00000684452.1:n.296G>T
ENST00000684632.1:n.348G>T
ENST00000566780.6:c.-32G>T MANE Select	ENSP00000457230.1:n.-32G>T
ENST00000355860.7:c.-32G>T	ENSP00000348119.3:n.-32G>T
ENST00000402655.6:c.-32G>T	ENSP00000384238.2:n.-32G>T
ENST00000406884.6:c.-32G>T	ENSP00000384495.2:n.-32G>T
ENST00000408984.7:c.-32G>T	ENSP00000386161.3:n.-32G>T
ENST00000539474.6:c.-32G>T	ENSP00000445210.2:n.-32G>T
ENST00000561846.5:n.13G>T
ENST00000562214.5:n.92G>T
ENST00000565562.5:n.14G>T
ENST00000566662.5:c.-32G>T	ENSP00000454331.1:n.-32G>T
ENST00000566780.5:c.-32G>T	ENSP00000457230.1:n.-32G>T
ENST00000569332.5:c.-32G>T	ENSP00000454788.1:n.-32G>T
ENST00000569818.1:c.-32G>T	ENSP00000454485.1:n.-32G>T
ENST00000627394.2:c.-32G>T	ENSP00000485925.1:n.-32G>T
NM_001291997.1:c.-306G>T	NP_001278926.1:n.-306G>T
NM_016373.3:c.-32G>T	NP_057457.1:n.-32G>T
NM_130791.3:c.-32G>T	NP_570607.1:n.-32G>T
NR_120435.1:n.335G>T
NR_120436.1:n.335G>T
XM_006721195.2:c.-32G>T	XP_006721258.1:n.-32G>T
XM_011523100.1:c.-32G>T	XP_011521402.1:n.-32G>T
XM_011523101.1:c.-32G>T	XP_011521403.1:n.-32G>T
XM_011523102.1:c.-32G>T	XP_011521404.1:n.-32G>T
XM_011523103.1:c.-32G>T	XP_011521405.1:n.-32G>T
XM_011523104.1:c.-32G>T	XP_011521406.1:n.-32G>T
XM_011523105.1:c.-32G>T	XP_011521407.1:n.-32G>T
XM_011523101.3:c.-32G>T	XP_011521403.1:n.-32G>T
XM_011523103.3:c.-32G>T	XP_011521405.1:n.-32G>T
XM_011523104.3:c.-32G>T	XP_011521406.1:n.-32G>T
XM_011523105.3:c.-32G>T	XP_011521407.1:n.-32G>T
XM_017023278.2:c.-32G>T	XP_016878767.1:n.-32G>T
NM_016373.4:c.-32G>T MANE Select	NP_057457.1:n.-32G>T
NM_001291997.2:c.-306G>T	NP_001278926.1:n.-306G>T
NM_130791.4:c.-32G>T	NP_570607.1:n.-32G>T
NR_120435.2:n.94G>T
NR_120436.2:n.94G>T
NM_130791.5:c.-32G>T	NP_570607.1:n.-32G>T
NR_120436.3:n.94G>T